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Clinical Trials in China / NCT07152756
Starting soon Observational

Impact of a One-Week Discontinuation of Semaglutide on Gastric Retention and Endoscopic Mucosal Visibility Scores

NCT07152756 · tracked via the Priya Life Science China tracker
Sponsor
Fudan University
Phase
Observational
Started
2025-09-15
Last updated
2025-09-03

Condition(s) studied

Gastric Retention

Investigational drug(s) / intervention(s)

Esophagogastroduodenoscopy

Esophagogastroduodenoscopy: Assess the gastric retention and the endoscopic mucosal visibility score during esophagogastroduodenoscopy

Study summary

A prospective, single-center, observational study to compare the risk of gastric retention and endoscopic mucosal visibility between the exposure group (one-week discontinuation of semaglutide before EGD) and non-exposure group (no semaglutide use before EGD)

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria 1. Subjects who have either: (i) been on long-term semaglutide therapy (≥4 weeks, any dosage) and discontinued use for one week prior to gastroscopy (with the last dose 8-14 days before the procedure), or(ii) never used semaglutide. 2. For patients with diabetes mellitus (DM), HbA1c \< 9% to ensure adequate glycemic control. 3. Age ≥ 18 years, with no restriction on sex. 4. American Society of Anesthesiologists (ASA) physical status classification I-II. 5. Fasting for at least 8 hours and no water intake for at least 4 hours before gastroscopy. 6. Undergoing painless (sedated) endoscopy. Exclusion Criteria 1. History of hiatal hernia or any previous gastric surgery (including gastrectomy, Roux-en-Y gastric bypass, etc.). 2. Pregnancy. 3. Medically unfit for gastrointestinal endoscopy. 4. Deemed unsuitable for participation at the discretion of the investigators.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Huadong hospital, Fudan university Shanghai Shanghai Municipality

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07152756 on ClinicalTrials.gov ↗ ← All trials in China